CTNNAL1
catenin alpha like 1
Summary
Predicted to enable actin filament binding activity and cadherin binding activity. Acts upstream of or within Rho protein signal transduction. Located in cytosol. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants42 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs761403846 | 9:111,706,042 | G/C | — | uncertain significance |
| rs1830316754 | 9:111,706,044 | G/A | — | uncertain significance |
| rs372641856 | 9:111,706,088 | G/C | — | uncertain significance |
| rs2537986396 | 9:111,706,261 | A/C | — | uncertain significance |
| rs1031600118 | 9:111,706,270 | G/A | — | uncertain significance |
| rs754763124 | 9:111,706,274 | G/A | — | uncertain significance |
| rs57784742 | 9:111,707,928 | G/T | downstream gene variant | — |
| rs536377756 | 9:111,714,557 | C/G | — | uncertain significance |
| rs1482381054 | 9:111,714,630 | A/G | — | uncertain significance |
| rs377052710 | 9:111,714,758 | A/T | — | uncertain significance |
| rs201571075 | 9:111,732,755 | T/C | — | uncertain significance |
| rs776203074 | 9:111,732,764 | A/G | — | uncertain significance |
| rs185777252 | 9:111,732,767 | C/T | — | uncertain significance |
| rs761895523 | 9:111,735,004 | A/C | — | uncertain significance |
| rs16913734 | 9:111,735,031 | G/C | — | benign |
| rs150783696 | 9:111,735,037 | T/G | — | uncertain significance |
| rs145040656 | 9:111,739,304 | C/T | — | uncertain significance |
| rs1268681619 | 9:111,741,610 | G/A | — | uncertain significance |
| rs142466437 | 9:111,741,679 | C/A | — | uncertain significance |
| rs200810664 | 9:111,741,689 | T/C | — | uncertain significance |
| rs140530317 | 9:111,745,483 | G/A | — | uncertain significance |
| rs774871628 | 9:111,745,505 | C/T | — | uncertain significance |
| rs138462885 | 9:111,745,535 | G/A | — | uncertain significance |
| rs755160373 | 9:111,745,559 | T/C | — | uncertain significance |
| rs994487558 | 9:111,745,595 | T/C | — | uncertain significance |
| rs201911236 | 9:111,749,466 | G/A | — | — |
| rs7026972 | 9:111,750,523 | T/C | downstream gene variant | — |
| rs923953725 | 9:111,754,920 | T/C | — | uncertain significance |
| rs912494476 | 9:111,754,949 | C/T | — | uncertain significance |
| rs753312528 | 9:111,755,058 | G/T | — | uncertain significance |
| rs116781162 | 9:111,761,469 | C/T | — | likely benign |
| rs1309947104 | 9:111,761,470 | G/A | — | uncertain significance |
| rs773605617 | 9:111,761,527 | G/A | — | uncertain significance |
| rs372154736 | 9:111,761,529 | G/A | — | uncertain significance |
| rs758644620 | 9:111,775,634 | A/G | — | uncertain significance |
| rs1827275263 | 9:111,775,638 | C/G | — | uncertain significance |
| rs2538105789 | 9:111,775,644 | C/G | — | uncertain significance |
| rs756612898 | 9:111,775,698 | C/T | — | uncertain significance |
| rs902973940 | 9:111,775,701 | C/T | — | uncertain significance |
| rs28361101 | 9:111,775,756 | G/C | regulatory region variant | — |
| rs28361098 | 9:111,776,195 | C/T | regulatory region variant | — |
| rs28361095 | 9:111,777,384 | C/T | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.